Temporal Variations of Global Fallout-Derived Plutonium And
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Hirose et al. Int J Earth Environ Sci 2016, 2: 125 https://doi.org/10.15344/2456-351X/2017/125 International Journal of Earth & Environmental Sciences Original Article Open Access Temporal Variations of Global Fallout-Derived Plutonium and 137Cs in River Water in Japan Katsumi Hirose1* and Michio Aoyama2 1Department of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, 7-1 Kioicho, Chiyodaku, Tokyo 102-8554, Japan 2Institute of Environmental Radioactivity, Fukushima University, 1 Kanayagawa, Fukushima 960-1296, Japan Abstract Publication History: Temporal variations of global fallout-derived plutonium and 137Cs concentrations in river water in Received: November 02, 2016 Japan were examined using a composite dataset for 1966–1987 (1966-1987 for 239,240Pu, 1978-1987 for Accepted: January 16, 2017 137Cs). Plutonium and 137Cs concentrations in Japanese river water exhibited exponential decreases Published: January 18, 2017 during the sampling periods, with the exception of 137Cs concentrations immediately after the Chernobyl Keywords: nuclear reactor accident in 1986. The apparent half-decrease time of dissolved 137Cs (1.9 ± 0.3 years), which means a time that radionuclide concentrations in river water decrease to a half, was similar to Plutonium, Radionuclides, 137Cs, that for dissolved 239,240Pu for the same period, whereas the apparent half-decrease time of particulate Japanese rivers 239,240Pu (4.5 ± 2.2years) was longer. Temporal changes in dissolved 239,240Pu and 137Cs in river water can be explained by direct contribution of radionuclides from rainwater and leaching of radionuclides from surface-layer soil particles on land. Introduction source of contamination of 137Cs and plutonium in major Japanese rivers except as a result of radioactive fallout originating from Plutonium and 137Cs released into the atmosphere by atmospheric atmospheric nuclear tests. The source of anthropogenic radionuclides testing of nuclear weapons and nuclear disasters involving nuclear in Japanese river water until 2011 is primarily global fallout from reactor accidents such as the Chernobyl nuclear reactor accident and atmospheric nuclear testing. Miyake and Tsubota [19] and Miyake Fukushima Daiichi Nuclear Power Plant (FDNPP) accident have been et al. [20] reported concentrations of 137Cs and plutonium in major deposited on land surfaces by both wet and dry deposition [1,2]. As a Japanese rivers and suggested that only a small portion of 137Cs and result of radioactive fallout from atmospheric nuclear tests, about 11 plutonium that was deposited on land surfaces is leached by river kBq m–2 and 44 Bq m–2 of 137Cs and 239,240Pu have been deposited on water because 137Cs and plutonium is tightly adsorbed on soil particles, land surfaces in Japan during 1945–1985 [3,4]. Most anthropogenic as shown by large partition coefficients for plutonium between soil radionuclides deposited on land surfaces were initially absorbed onto particles and the aqueous phase [21]. surface soil particles, although adsorption reactions between soil particles and radionuclides differ between radionuclides; typically The dynamics of chemical constituents, including radionuclides, plutonium reacts with biogenic organic matter including micro trace metals, and nutrients, are often complex in river systems [22]. organisms [5-7], whereas radiocesium adsorbs onto clay minerals River water comes from three sources: overland flow, groundwater, [8-11]. Subsequently, the anthropogenic radionuclides gradually and subsurface stormflow. Precipitation plays an especially important migrated within terrestrial environments. A portion of radionuclides role in overland flow. Chemical and biological interactions that in terrestrial environments was transported into the ocean via control element concentrations vary among rivers, as does the source river runoff and aeolian processes involving radionuclide-bearing of river water. Although complex chemical processes occur in rivers, dust particles [12]. After the 1986 Chernobyl and 2011 FDNPP a major process in river systems is the leaching of elements from the accidents, migration of anthropogenic radionuclides in the terrestrial land surface [22-24]. Precipitation is another important factor because environment has been major concern to assess radiological effects, in it is a direct source of anthropogenic radionuclides, as shown by the which river runoff of the anthropogenic radionuclides are one of the increase in 137Cs concentrations in river water immediately after the most important processes [6,11,13,14]. Chernobyl accident [21]. However, factors controlling anthropogenic radionuclides in rivers remain poorly understood. Before these In order to have better understanding of the long-term river runoff factors can be examined, however, temporal variations of the global processes of anthropogenic radionuclides, it is necessary to have fallout-derived 137Cs and 239,240Pu concentrations in major Japanese long-term monitoring results of concentrations of anthropogenic rivers must be analyzed. However, little information is available on radionuclides in river water. Monitoring results for anthropogenic long-term variations of the 137Cs and 239,240Pu concentrations in river radionuclides derived from atmospheric nuclear explosions would water because of a lack of long-term monitoring of anthropogenic provide a good opportunity to study the long-term riverine processes. radionuclides in rivers. Except the large-scale nuclear reactor accidents, most of the 137Cs *Corresponding Author: Prof. Katsumi Hirose, Department of Materials and Life 239,240 Sciences, Faculty of Science and Technology, Sophia University, 7-1 Kioicho, and Pu in river water originated from global fallout, although Chiyodaku, Tokyo 102-8554, Japan; E-mail: [email protected] anthropogenic radionuclides have been discharged into several rivers from nuclear facilities, including nuclear reactors and nuclear Citation: Hirose K, Aoyama M (2017) Temporal variations of global fallout- 137 fuel reprocessing plants. In this connection, concentrations of derived plutonium and Cs in river water in Japan. Int J Earth Environ Sci 2: 125. doi: https://doi.org/10.15344/2456-351X/2017/125 anthropogenic radionuclides in river water have been determined so that the effects of radioactive discharge from nuclear facilities can be Copyright: © 2017 Hirose. This is an open-access article distributed under the assessed [15-18]. In Japan, most nuclear facilities are located in coastal terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author areas. Therefore, until the 2011 FDNPP accident, there is no obvious and source are credited. Int J Earth Environ Sci IJEES, an open access journal ISSN: 2456-351X Volume 1. 2017. 125 Citation: Hirose K, Aoyama M (2017) Temporal variations of global fallout-derived plutonium and 137Cs in river water in Japan. Int J Earth Environ Sci 2: 125. doi: https://doi.org/10.15344/2456-351X/2017/125 Page 2 of 7 In this paper, we report data obtained in Environmental Radiation (Kyushu Island) rivers. Locations and sampling sites are shown Survey (ERS) project, Japan and examine the temporal variation in Figure 2. Sampling period of each river is shown in Table 1. The in previously reported 137Cs and 239,240Pu concentrations in major sampling site on each river was selected to avoid industrial and urban Japanese rivers[20,25] in order to elucidate behaviors of global fallout- pollution as well as inflowing seawater. A water sample of 1000 L derived radionuclides in the terrestrial environment. was collected from each river. The water was filtered through a fine membrane filter (Millipore HA, pore size of 0.45 μm and diameter of Background 293 mm) immediately after collection. Meteorological Research Institute (MRI) have conducted the ERS project since 1957 to monitor the environmental effects of anthropogenic radionuclides derived from atmospheric nuclear testing. This project revealed temporal changes of deposition fluxes of anthropogenic radionuclides due to global fallout; the maximum deposition fluxes of 137Cs and 239,240Pu occurred in 1963 after the large- scale US and former USSR atmospheric nuclear tests in 1961-62, and although since Nuclear Test-Ban Treaty in 1963 these deposition fluxes decreased exponentially according to the stratospheric residence time of radioactive aerosols, the radioactive deposition fluxes varied due to Chinese atmospheric nuclear tests conducted until 1980 [2,3]. Terrestrial environment was contaminated by deposition of the anthropogenic radionuclides from global fallout [26]. It is important to assess the effects of the anthropogenic radionuclides in the terrestrial environment. MRI had conducted the research project entitled Behavior of Transuranic Elements in the Environment during the period of 1978 – 1988, in which 137Cs and 239,240Pu concentrations in major rivers in Japan were measured. Figure 1 shows the temporal variations of annual deposition fluxes of 137Cs and 239,240Pu observed at Tsukuba, Japan during the period of 1978 – 1988, in which the annual 137Cs and 239,240Pu deposition fluxes, ranged from 0.067 (in 1985) to 135 Bq m-2y-1 (in 1986) and from 0.026 (in 1985) to 0.27 Bq m-2y-1 (in 1977), respectively varied more than one order of magnitude. Figure 2: Locations and sampling sites for 24 rivers in Japan. 1., Ishikari; 2., Omono; 3., Kitakami; 4., Mogami; 5., Shinano; 6., Tone; 7., Fuji; 8., Tenryu; 9., Kiso; 10., Kuzuryu; 11., Yodo; 12., Asahi; 13., Gou; 14., Hii; 15., Ohota; 16., Yoshino; 17., Chikugo; 18., Ohono; 19., Sendai; 20., Kuma; 21., Ohyodo; 22., Gokase; 23., Yura; and 24., Teshio. Name of Sampling 239,240Pu (mBq m–3) Dissolved river time 137Cs (Bq m–3) Dissolved Particulate Kitakami Aug. 1966 25±3 a 21±2 a Mogami Aug. 1966 67±4 a 21±2 a Shinano Oct. 1966 8.5±0.7 a 14±1 a Kiso Oct. 1966 19±2 a 11±1 a Tone Nov. 1966 154±7 a 7.8±0.7 a Yodo Aug. 1967 2.6±0.4 a 4.8±0.4 a a a Figure 1: Temporal variations of annual deposition fluxes of 137Cs and Asahi Aug. 1967 9.6±0.7 8.5±0.7 239,240Pu observed at Tokyo (1986 - 1980) and Tsukuba (1980 - ). Red Yoshino Aug.